Department of Endocrinology, University of Ioannina, Ioannina, Greece.
Hum Reprod. 2010 Dec;25(12):3129-33. doi: 10.1093/humrep/deq276. Epub 2010 Oct 11.
Twin studies have shown that age at menarche may be subject to hereditary influences but the specific determinants are unknown. Estrogens are known to have an important role in menarche. Since the enzyme aromatase is responsible for the conversion of androgens to estrogens, the aromatase (CYP19) gene could be a candidate gene for the regulation of menarche. The aim of this study was to investigate the possible association of the CYP19(TTTA)(n) polymorphism with age at menarche.
We studied 130 healthy adolescent females from a closed community in North-Western Greece. Information on menarche was obtained through interviews. The BMI was recorded. The CYP19(TTTA)(n) polymorphism was genotyped.
The mean age at menarche was 12.9 ± 1.2 years and the BMI = 19.8 ± 2.3 kg/m(2). Genotype analysis revealed 5 CYP19(TTTA)(n) alleles containing 7-11 TTTA repeats. Girls homozygous for the allele with 7 TTTA repeats had earlier menarche (12.45 ± 0.9 years) than girls carrying other genotypes (13.0 ± 1.2 years, P = 0.025), whereas the BMI was not different between these two subgroups. Carriers of the allele with 11 TTTA repeats had later menarche compared with non-carriers (14.1 ± 0.75 versus 12.8 ± 1.2 years, P< 0.001), whereas no difference was found in BMI values. Comparing girls with early menarche (<12 years, 25th percentile) with girls with late menarche (>13.75 years, 75th percentile), we found that 31% of the girls with early menarche were homozygous for the (TTTA)(7) allele compared with 6.9% among girls with late menarche (P = 0.018). In addition, none of the girls carrying the (TTTA)(11) allele was found among the subgroup with early menarche, whereas 24.1% of girls with late menarche had the (TTTA)(11) allele (P = 0.001). No association between other alleles and age at menarche was found.
There is evidence for a genetic contribution of the CYP19 gene to the age at menarche.
双胞胎研究表明,初潮年龄可能受到遗传因素的影响,但具体的决定因素尚不清楚。雌激素在初潮中起着重要作用。由于芳香酶负责将雄激素转化为雌激素,因此芳香酶(CYP19)基因可能是调节初潮的候选基因。本研究旨在探讨 CYP19(TTTA)(n) 多态性与初潮年龄的可能相关性。
我们研究了来自希腊西北部一个封闭社区的 130 名健康青春期女性。通过访谈获得初潮信息。记录 BMI。对 CYP19(TTTA)(n) 多态性进行了基因分型。
初潮年龄的平均值为 12.9 ± 1.2 岁,BMI = 19.8 ± 2.3 kg/m(2)。基因型分析显示,有 5 种 CYP19(TTTA)(n) 等位基因,包含 7-11 个 TTTA 重复。携带 7 个 TTTA 重复的等位基因纯合子的女孩初潮较早(12.45 ± 0.9 岁),而携带其他基因型的女孩初潮较晚(13.0 ± 1.2 岁,P = 0.025),而这两个亚组的 BMI 没有差异。携带 11 个 TTTA 重复的等位基因的携带者比非携带者的初潮较晚(14.1 ± 0.75 岁与 12.8 ± 1.2 岁,P< 0.001),而 BMI 值没有差异。将初潮较早(<12 岁,第 25 百分位数)的女孩与初潮较晚(>13.75 岁,第 75 百分位数)的女孩进行比较,我们发现,在初潮较早的女孩中,有 31%是纯合子(TTTA)(7)等位基因,而在初潮较晚的女孩中,只有 6.9%是纯合子(TTTA)(P = 0.018)。此外,在初潮较早的亚组中没有发现携带(TTTA)(11)等位基因的女孩,而在初潮较晚的女孩中,有 24.1%携带(TTTA)(11)等位基因(P = 0.001)。没有发现其他等位基因与初潮年龄之间存在关联。
CYP19 基因对初潮年龄有遗传贡献的证据。